Canonical Allele Identifier: CA362032982
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320488G>T , CM000667.2:g.159320488G>T GRCh38
NC_000005.9:g.158747496G>T , CM000667.1:g.158747496G>T GRCh37
NC_000005.8:g.158680074G>T NCBI36
NG_009618.1:g.14986C>A , LRG_71:g.14986C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-116C>A ENSP00000512849.1:n.-116C>A
ENST00000696751.1:c.*10C>A ENSP00000512850.1:n.*10C>A
ENST00000231228.3:c.515C>A MANE Select ENSP00000231228.2:p.Ala172Asp
ENST00000231228.2:c.515C>A ENSP00000231228.2:p.Ala172Asp
NM_002187.2:c.515C>A , LRG_71t1:c.515C>A NP_002178.2:p.Ala172Asp
XR_001742945.1:n.39G>T
NM_002187.3:c.515C>A MANE Select NP_002178.2:p.Ala172Asp